Canonical Allele Identifier: CA1573465750
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112842576T= , CM000667.2:g.112842576T= GRCh38
NC_000005.9:g.112178273T= , CM000667.1:g.112178273T= GRCh37
NC_000005.8:g.112206172T= NCBI36
NG_008481.4:g.155056T= , LRG_130:g.155056T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7036T= ENSP00000473355.2:p.Ser2346=
ENST00000505350.2:c.*6988T= ENSP00000481752.1:n.*6988T=
ENST00000507379.6:c.6928T= ENSP00000423224.2:p.Ser2310=
ENST00000509732.6:c.6982T= ENSP00000426541.2:p.Ser2328=
ENST00000512211.7:c.6982T= ENSP00000423828.3:p.Ser2328=
ENST00000257430.9:c.6982T= MANE Select ENSP00000257430.4:p.Ser2328=
ENST00000257430.8:c.6982T= ENSP00000257430.4:p.Ser2328=
ENST00000508376.6:c.6982T= ENSP00000427089.2:p.Ser2328=
ENST00000508624.5:c.*6304T= ENSP00000424265.1:n.*6304T=
ENST00000520401.1:c.230+13604T=
NM_000038.5:c.6982T= NP_000029.2:p.Ser2328=
NM_001127510.2:c.6982T= NP_001120982.1:p.Ser2328=
NM_001127511.2:c.6928T= NP_001120983.2:p.Ser2310=
NM_001354895.1:c.6982T= NP_001341824.1:p.Ser2328=
NM_001354896.1:c.7036T= NP_001341825.1:p.Ser2346=
NM_001354897.1:c.7012T= NP_001341826.1:p.Ser2338=
NM_001354898.1:c.6907T= NP_001341827.1:p.Ser2303=
NM_001354899.1:c.6898T= NP_001341828.1:p.Ser2300=
NM_001354900.1:c.6859T= NP_001341829.1:p.Ser2287=
NM_001354901.1:c.6805T= NP_001341830.1:p.Ser2269=
NM_001354902.1:c.6709T= NP_001341831.1:p.Ser2237=
NM_001354903.1:c.6679T= NP_001341832.1:p.Ser2227=
NM_001354904.1:c.6604T= NP_001341833.1:p.Ser2202=
NM_001354905.1:c.6502T= NP_001341834.1:p.Ser2168=
NM_001354906.1:c.6133T= NP_001341835.1:p.Ser2045=
NM_000038.6:c.6982T= MANE Select NP_000029.2:p.Ser2328=
NM_001127510.3:c.6982T= NP_001120982.1:p.Ser2328=
NM_001127511.3:c.6928T= NP_001120983.2:p.Ser2310=
NM_001354895.2:c.6982T= NP_001341824.1:p.Ser2328=
NM_001354896.2:c.7036T= NP_001341825.1:p.Ser2346=
NM_001354897.2:c.7012T= NP_001341826.1:p.Ser2338=
NM_001354898.2:c.6907T= NP_001341827.1:p.Ser2303=
NM_001354899.2:c.6898T= NP_001341828.1:p.Ser2300=
NM_001354900.2:c.6859T= NP_001341829.1:p.Ser2287=
NM_001354901.2:c.6805T= NP_001341830.1:p.Ser2269=
NM_001354902.2:c.6709T= NP_001341831.1:p.Ser2237=
NM_001354903.2:c.6679T= NP_001341832.1:p.Ser2227=
NM_001354904.2:c.6604T= NP_001341833.1:p.Ser2202=
NM_001354905.2:c.6502T= NP_001341834.1:p.Ser2168=
NM_001354906.2:c.6133T= NP_001341835.1:p.Ser2045=